Colon Cancer: Gene >> IGF1R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98939336:98939336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769418210
CDS Mutation	c.3433G>A
AA Mutation	p.Glu1145Lys(p.E1145K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98922344:98922344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2398C>T
AA Mutation	p.Arg800Cys(p.R800C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98929602:98929602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761063787
CDS Mutation	c.2827G>A
AA Mutation	p.Ala943Thr(p.A943T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98913186:98913186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1732G>A
AA Mutation	p.Ala578Thr(p.A578T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98911363:98911363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761469469
CDS Mutation	c.1511G>A
AA Mutation	p.Arg504His(p.R504H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98948602:98948602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772355972
CDS Mutation	c.3616G>A
AA Mutation	p.Ala1206Thr(p.A1206T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98934991:98934991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3124C>T
AA Mutation	p.Arg1042Cys(p.R1042C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98708077:98708077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610C>T
AA Mutation	p.Arg204Cys(p.R204C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98708094:98708094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627C>A
AA Mutation	p.Asn209Lys(p.N209K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98913123:98913123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1669C>T
AA Mutation	p.Pro557Ser(p.P557S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98916028:98916028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1893G>T
AA Mutation	p.Trp631Cys(p.W631C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98707789:98707789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322G>A
AA Mutation	p.Gly108Ser(p.G108S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98908700:98908700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542546475
CDS Mutation	c.1263C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98911424:98911424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757261009
CDS Mutation	c.1572C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98930295:98930295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2946C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98916775:98916775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767179117
CDS Mutation	c.2100C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98707668:98707668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45468203
CDS Mutation	c.201C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268035
Start	98899580:98899580(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1211delA
AA Mutation	p.Asn404ThrfsTer6(p.N404Tfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000268035
Start	98942937:98942937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3472C>T
AA Mutation	p.Arg1158Ter(p.R1158*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IGF1R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268035
Start	98916741:98916741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2066C>T
AA Mutation	p.Thr689Ile(p.T689I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98908883:98908883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537098180
CDS Mutation	c.1446C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98896886:98896886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1083C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268035
Start	98939356:98939356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375579623
CDS Mutation	c.3453C>T
Mutation Classification	Silent
Feature Type	Transcript